Canonical Allele Identifier: CA1964082487
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1856913720

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350215del , CM000673.2:g.36350215del GRCh38
NC_000011.9:g.36371765del , CM000673.1:g.36371765del GRCh37
NC_000011.8:g.36328341del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50782del MANE Select ENSP00000435050.1:n.-125-50782del
ENST00000527172.5:c.-291-43631del ENSP00000433708.1:n.-291-43631del
ENST00000529034.5:n.152-50782del
ENST00000530639.5:c.-125-50782del ENSP00000435050.1:n.-125-50782del
ENST00000532121.5:c.-126+150del ENSP00000433893.1:n.-126+150del
NM_001160167.1:c.-125-50782del NP_001153639.1:n.-125-50782del
NM_001160167.2:c.-125-50782del MANE Select NP_001153639.1:n.-125-50782del